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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Class Implantable

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MaXcess - 00887517650061

MaXcess MAS TLIF Blade, 60mm C-C
Nuvasive, Inc.
3500103
In Commercial Distribution

  • 00887517650061 ()


  • Surgical retraction system, reusable

MaXcess - 00887517650054

MaXcess MAS TLIF Blade, 50mm C-C
Nuvasive, Inc.
3500102
In Commercial Distribution

  • 00887517650054 ()


  • Surgical retraction system, reusable

MaXcess - 00887517650047

MaXcess MAS TLIF Blade, 40mm C-C
Nuvasive, Inc.
3500101
In Commercial Distribution

  • 00887517650047 ()


  • Surgical retraction system, reusable

MaXcess - 00887517649980

MaXcess MAS TLIF Base, Blade Ster Case
Nuvasive, Inc.
3500091
In Commercial Distribution

  • 00887517649980 ()


  • Device sterilization/disinfection container, reusable

MaXcess - 00887517649911

MaXcess MAS TLIF Base, Ster Case
Nuvasive, Inc.
3500081
In Commercial Distribution

  • 00887517649911 ()


  • Device sterilization/disinfection container, reusable

MaXcess - 00887517649904

MaXcess MAS TLIF Medial Rack, Double
Nuvasive, Inc.
3500050
In Commercial Distribution

  • 00887517649904 ()


  • Surgical retraction system, reusable

MaXcess - 00887517649898

MaXcess MAS TLIF Medial Rack, Single
Nuvasive, Inc.
3500040
In Commercial Distribution

  • 00887517649898 ()


  • Surgical retraction system, reusable

MaXcess - 00887517649874

MaXcess MAS TLIF Blade, Medial XL
Nuvasive, Inc.
3500035
In Commercial Distribution

  • 00887517649874 ()


  • Surgical retraction system, reusable

MaXcess - 00887517649867

MaXcess MAS TLIF Blade, Medial Large
Nuvasive, Inc.
3500034
In Commercial Distribution

  • 00887517649867 ()


  • Surgical retraction system, reusable

MaXcess - 00887517649850

MaXcess MAS TLIF Blade, Medial Med
Nuvasive, Inc.
3500033
In Commercial Distribution

  • 00887517649850 ()


  • Surgical retraction system, reusable
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